Canonical Allele Identifier: CA2501215771
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780555_214780556insT , CM000664.2:g.214780555_214780556insT GRCh38
NC_000002.11:g.215645279_215645280insT , CM000664.1:g.215645279_215645280insT GRCh37
NC_000002.10:g.215353524_215353525insT NCBI36
NG_012047.2:g.34149_34150insA
NG_012047.3:g.34156_34157insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1314+4_1314+5insA MANE Select ENSP00000260947.4:n.1314+4_1314+5insA
ENST00000421162.2:c.215+16505_215+16506insA ENSP00000392245.2:n.215+16505_215+16506insA
ENST00000613192.2:c.158+28856_158+28857insA ENSP00000483275.2:n.158+28856_158+28857insA
ENST00000613374.5:c.159-28001_159-28000insA ENSP00000484464.1:n.159-28001_159-28000insA
ENST00000613706.5:c.906+412_906+413insA ENSP00000484976.2:n.906+412_906+413insA
ENST00000617164.5:c.1257+4_1257+5insA ENSP00000480470.1:n.1257+4_1257+5insA
ENST00000619009.5:c.364+11741_364+11742insA ENSP00000482293.1:n.364+11741_364+11742insA
ENST00000650978.1:c.1156+4_1156+5insA
ENST00000260947.8:c.1314+4_1314+5insA ENSP00000260947.4:n.1314+4_1314+5insA
ENST00000421162.1:c.215+16505_215+16506insA ENSP00000392245.1:n.215+16505_215+16506insA
ENST00000455743.5:c.*934+4_*934+5insA ENSP00000412186.1:n.*934+4_*934+5insA
ENST00000613192.1:c.73+28856_73+28857insA ENSP00000483275.1:n.73+28856_73+28857insA
ENST00000613374.4:c.159-28001_159-28000insA ENSP00000484464.1:n.159-28001_159-28000insA
ENST00000613706.4:c.215+16505_215+16506insA ENSP00000484976.1:n.215+16505_215+16506insA
ENST00000617164.4:c.1257+4_1257+5insA ENSP00000480470.1:n.1257+4_1257+5insA
ENST00000619009.4:c.364+11741_364+11742insA ENSP00000482293.1:n.364+11741_364+11742insA
ENST00000620057.4:c.365-11244_365-11243insA ENSP00000481988.1:n.365-11244_365-11243insA
NM_000465.3:c.1314+4_1314+5insA NP_000456.2:n.1314+4_1314+5insA
NM_001282543.1:c.1257+4_1257+5insA NP_001269472.1:n.1257+4_1257+5insA
NM_001282545.1:c.215+16505_215+16506insA NP_001269474.1:n.215+16505_215+16506insA
NM_001282548.1:c.159-28001_159-28000insA NP_001269477.1:n.159-28001_159-28000insA
NM_001282549.1:c.364+11741_364+11742insA NP_001269478.1:n.364+11741_364+11742insA
NR_104212.1:n.1307+4_1307+5insA
NR_104215.1:n.1250+4_1250+5insA
NR_104216.1:n.507-11244_507-11243insA
XM_011511567.1:c.1260+4_1260+5insA XP_011509869.1:n.1260+4_1260+5insA
XM_011511568.1:c.1314+4_1314+5insA XP_011509870.1:n.1314+4_1314+5insA
XM_017004613.1:c.1413+4_1413+5insA XP_016860102.1:n.1413+4_1413+5insA
XM_017004614.1:c.1413+4_1413+5insA XP_016860103.1:n.1413+4_1413+5insA
XR_002959322.1:n.1504+4_1504+5insA
NM_000465.4:c.1314+4_1314+5insA MANE Select NP_000456.2:n.1314+4_1314+5insA
NM_001282543.2:c.1257+4_1257+5insA NP_001269472.1:n.1257+4_1257+5insA
NM_001282545.2:c.215+16505_215+16506insA NP_001269474.1:n.215+16505_215+16506insA
NM_001282548.2:c.159-28001_159-28000insA NP_001269477.1:n.159-28001_159-28000insA
NM_001282549.2:c.364+11741_364+11742insA NP_001269478.1:n.364+11741_364+11742insA
NR_104212.2:n.1279+4_1279+5insA
NR_104215.2:n.1222+4_1222+5insA
NR_104216.2:n.479-11244_479-11243insA